Optimized CRISPR/Cas tools for efficient germline and somatic genome engineering in Drosophila

A Programmable Dual-RNA–Guided DNA Endonuclease in Adaptive Bacterial Immunity

Jinek, M., Chylinski, K., Fonfara, I., Hauer, M., Doudna, J. A., & Charpentier, E. (2012) · Science · doi:10.1126/science.1225829 · Cited by 17,116

Targeted gene expression as a means of altering cell fates and generating dominant phenotypes

Brand, A. H., & Perrimon, N. (1993) · Development · doi:10.1242/dev.118.2.401 · Cited by 9,510

RNA-Guided Human Genome Engineering via Cas9

Mali, P., Yang, L., Esvelt, K. M., Aach, J., Guell, M., DiCarlo, J. E., Norville, J. E., & Church, G. M. (2013) · Science · doi:10.1126/science.1232033 · Cited by 9,210

Mutations affecting segment number and polarity in Drosophila

Nüsslein‐Volhard, C., & Wieschaus, E. F. (1980) · Nature · doi:10.1038/287795a0 · Cited by 4,370

One-step generation of mice carrying mutations in multiple genes by CRISPR/Cas-mediated genome engineering

Wang, H., Yang, H., Shivalila, C. S., Dawlaty, M. M., Cheng, A. W., Zhang, F., & Jaenisch, R. (2013) · Cell · doi:10.1016/j.cell.2013.04.025 · Cited by 3,495

Double nicking by RNA-guided CRISPR Cas9 for enhanced genome editing specificity

Ran, F. A., Hsu, P. D., Lin, C.-Y., Gootenberg, J. S., Konermann, S., Trevino, A. E., Scott, D. A., Inoue, A., Matoba, S., Zhang, Y., et al. (2013) · Cell · doi:10.1016/j.cell.2013.08.021 · Cited by 3,299

High-Frequency off-Target Mutagenesis Induced by CRISPR-Cas Nucleases in Human Cells

Fu, Y., Foden, J. A., Khayter, C., Maeder, M. L., Reyon, D., Joung, J. K., & Sander, J. D. (2013) · Nature Biotechnology · doi:10.1038/nbt.2623 · Cited by 3,292

RNA-programmed genome editing in human cells

Jinek, M., East, A., Cheng, A., Lin, S., Ma, E., & Doudna, J. (2013) · eLife · doi:10.7554/elife.00471 · Cited by 2,098

Improving CRISPR-Cas nuclease specificity using truncated guide RNAs

Fu, Y., Sander, J. D., Reyon, D., Cascio, V. M., & Joung, J. K. (2014) · Nature Biotechnology · doi:10.1038/nbt.2808 · Cited by 1,993 · cited 1×

An optimized transgenesis system for Drosophila using germ-line-specific φC31 integrases

Bischof, J., Maeda, R., Hediger, M., Karch, F., & Basler, K. (2007) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.0611511104 · Cited by 1,959

Wampa is a dynein subunit required for axonemal assembly and male fertility in Drosophila

Bauerly, E., Yi, K., & Gibson, M. C. (2020) · Developmental Biology · doi:10.1016/j.ydbio.2020.04.006 · Cited by 14

Functional Divergence of the bag-of-marbles Gene in the Drosophila melanogaster Species Group

Bubnell, J. E., Ulbing, C. K. S., Begne, P. F., & Aquadro, C. F. (2022) · Molecular Biology and Evolution · doi:10.1093/molbev/msac137 · Cited by 14

Functional and Genetic Analysis of Spectraplakins in Drosophila

Hahn, I., Ronshaugen, M., Sánchez‐Soriano, N., & Prokop, A. (2015) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/bs.mie.2015.06.022 · Cited by 14

The Hox Transcription Factor Ubx Ensures Somatic Myogenesis by Suppressing the Mesodermal Master Regulator Twist

Domsch, K., Schröder, J., Janeschik, M., Schaub, C., & Lohmann, I. (2021) · Cell Reports · doi:10.1016/j.celrep.2020.108577 · Cited by 14

Lessons in genome engineering: opportunities, tools and pitfallsPreprint

Poernbacher, I., Crossman, S. H., Kurth, J., Nojima, H., Baena-López, L. A., Alexandre, C., & Vincent, J. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/710871 · Cited by 14

TM2D genes regulate Notch signaling and neuronal function in Drosophila

Salazar, J. L., Yang, S.-A., Lin, Y. Q., Li-Kroeger, D., Marcogliese, P. C., Deal, S. L., Neely, G. G., & Yamamoto, S. (2021) · PLOS Genetics · doi:10.1371/journal.pgen.1009962 · Cited by 13

Stem-loop and circle-loop TADs generated by directional pairing of boundary elements have distinct physical and regulatory properties

Ke, W., Fujioka, M., Schedl, P. D., & Jaynes, J. B. (2024) · eLife · doi:10.7554/elife.94114 · Cited by 23

Seamless knockins in Drosophila via CRISPR-triggered single-strand annealing

Aguilar, G., Bauer, M., Viganò, M., Schnider, S. T., Brügger, L., Jiménez‐Jiménez, C., Guerrero, I., & Affolter, M. (2024) · Developmental Cell · doi:10.1016/j.devcel.2024.06.004 · Cited by 13

A genetic screen in Drosophila uncovers a role for senseless-2 in surface glia in the peripheral nervous system to regulate CNS morphology

Lacin, H., Zhu, Y., DiPaola, J. T., Wilson, B. A., Zhu, Y., & Skeath, J. B. (2024) · G3 Genes Genomes Genetics · doi:10.1093/g3journal/jkae152 · Cited by 14

Higher resolution pooled genome-wide CRISPR knockout screening in Drosophila cells using integration and anti-CRISPR (IntAC)

Viswanatha, R., Entwisle, S., Hu, Y.-H., Kim, A.-R., Reap, K., Butnaru, M., Qadiri, M., Mohr, S. E., & Perrimon, N. (2025) · Nature Communications · doi:10.1038/s41467-025-61692-3 · Cited by 7

Sensitized genetic backgrounds reveal differential roles for EGF repeat xylosyltransferases in Drosophila Notch signaling

Pandey, A. N., Li‐Kroeger, D., Sethi, M. K., Lee, T. V., Buettner, F. F. R., Bakker, H., & Jafar‐Nejad, H. (2018) · Glycobiology · doi:10.1093/glycob/cwy080 · Cited by 13

Dopamine modulates the optomotor response to unreliable visual stimuli in Drosophila melanogaster

Akiba, M., Sugimoto, K., Aoki, R., Murakami, R., Miyashita, T., Hashimoto, R., Hiranuma, A., Yamauchi, J., Ueno, T., & Morimoto, T. (2019) · European Journal of Neuroscience · doi:10.1111/ejn.14648 · Cited by 13

Generating and testing the efficacy of transgenic Cas9 in Tribolium castaneum

Rylee, J. C., Nin-Velez, A., Mahato, S., Helms, K. J., Wade, M. J., Zentner, G. E., & Zelhof, A. C. (2022) · Insect Molecular Biology · doi:10.1111/imb.12778 · Cited by 13

Use of Insect Promoters in Genetic Engineering to Control Mosquito-Borne Diseases

Bottino-Rojas, V., & James, A. A. (2022) · Biomolecules · doi:10.3390/biom13010016 · Cited by 13

Mob4 is essential for spermatogenesis in Drosophila melanogaster

Santos, I. B., Wainman, A., Garrido‐Maraver, J., Pires, V., Riparbelli, M. G., Kovács, L., Callaini, G., Glover, D. M., & Tavares, Á. A. (2023) · Genetics · doi:10.1093/genetics/iyad104 · Cited by 13

An optimized TALEN application for mutagenesis and screening inDrosophila melanogaster

Lee, H. B., Sebo, Z. L., Peng, Y., & Guo, Y. (2015) · Cellular Logistics · doi:10.1080/21592799.2015.1023423 · Cited by 13

T cell-specific inactivation of mouse CD2 by CRISPR/Cas9

Beil-Wagner, J., Dössinger, G., Schober, K., Berg, J. V., Tresch, A., Grandl, M., Palle, P., Mair, F., Gerhard, M., Becher, B., et al. (2016) · Scientific Reports · doi:10.1038/srep21377 · Cited by 13

TheDrosophila Retgene functions in the stomatogastric nervous system with the Maverick TGFβ ligand and theGfrlco-receptor

Myers, L. G., Perera, H., Alvarado, M. G., & Kidd, T. (2017) · Development · doi:10.1242/dev.157446 · Cited by 13

Parallel Genomic Engineering of Two Drosophila Genes Using Orthogonal attB/attP Sites

Blanco-Redondo, B., & Langenhan, T. (2018) · G3 Genes Genomes Genetics · doi:10.1534/g3.118.200565 · Cited by 13

Molecular tools to create new strains for mosquito sexing and vector control

Häcker, I., & Schetelig, M. F. (2018) · Parasites & Vectors · doi:10.1186/s13071-018-3209-6 · Cited by 13

Two modes of transvection at the eyes absent gene of Drosophila demonstrate plasticity in transcriptional regulatory interactions in cis and in trans

Tian, K., Henderson, R. E., Parker, R., Brown, A., Johnson, J. E., & Bateman, J. R. (2019) · PLoS Genetics · doi:10.1371/journal.pgen.1008152 · Cited by 13

F654A and K558Q Mutations in NMDA Receptor 1 Affect Ethanol‐Induced Behaviors in Drosophila

Troutwine, B., Park, A., Vélez-Hernández, M. E., Lew, L. K., Mihic, S. J., & Atkinson, N. S. (2019) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.14215 · Cited by 13

Tissue specific requirement of Drosophila Rcd4 for centriole duplication and ciliogenesis

Panda, P., Kovács, L., Dzhindzhev, N. S., Fatalska, A., Persico, V., Geymonat, M., Riparbelli, M. G., Callaini, G., & Glover, D. M. (2020) · The Journal of Cell Biology · doi:10.1083/jcb.201912154 · Cited by 13

Efficient nanoparticle‐based CRISPR‐Cas13d induced mRNA disruption of an eye pigmentation gene in the white‐backed planthopper, Sogatella furcifera

Ma, Y., Zhang, M., Gong, L., Liu, X., Long, G., Guo, H., Hull, J. J., Dewer, Y., He, M., & He, P. (2023) · Insect Science · doi:10.1111/1744-7917.13203 · Cited by 12

Modular vector assembly enables rapid assessment of emerging CRISPR technologies

McGee, A. V., Liu, Y. V., Griffith, A. L., Szegletes, Z. M., Wen, B., Kraus, C., Miller, N. W., Steger, R. J., Velasco, B. E., Bosch, J. A., et al. (2024) · Cell Genomics · doi:10.1016/j.xgen.2024.100519 · Cited by 12

Epg5 links proteotoxic stress due to defective autophagic clearance and epileptogenesis in Drosophila and Vici syndrome patients

Deneubourg, C., Dafsari, H. S., Lowe, S. A., Martinez-Cotrina, A., Mazaud, D., Park, S. H., Vergani, V., Almacellas‐Barbanoj, A., Maroofian, R., Averdunk, L., et al. (2024) · Autophagy · doi:10.1080/15548627.2024.2405956 · Cited by 13

Wingless strain created using binary transgenic CRISPR/Cas9 alleviates concerns about mass rearing of Hermetia illucens

Kou, Z., Wang, S., Luo, X., Xu, J. Q., Tomberlin, J. K., & Huang, Y. (2024) · Communications Biology · doi:10.1038/s42003-024-07254-7 · Cited by 12

Escalation of genome defense capacity enables control of an expanding meiotic driver

Chen, P., Pan, K. C., Park, E. H., Luo, Y., Lee, Y. C. G., & Aravin, A. A. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2418541122 · Cited by 14

Developmental axon regrowth and primary neuron sprouting utilize distinct actin elongation factors

Yaniv, S. P., Meltzer, H., Alyagor, I., & Schuldiner, O. (2020) · The Journal of Cell Biology · doi:10.1083/jcb.201903181 · Cited by 12

Enhanced Golic+: highly effective CRISPR gene targeting and transgene HACKing in Drosophila

Chen, H.-M., Yao, X., Ren, Q., Chang, C.-C., Liu, L., Miyares, R. L., & Lee, T. (2020) · Development · doi:10.1242/dev.181974 · Cited by 12

Intrinsic control of muscle attachment sites matching

Carayon, A., Bataillé, L., Lebreton, G., Dubois, L., Pelletier, A., Carrier, Y., Wystrach, A., Vincent, A., & Frendo, J. (2020) · eLife · doi:10.7554/elife.57547 · Cited by 13

Drosophila USP22/nonstop polarizes the actin cytoskeleton during collective border cell migration

Badmos, H. A., Cobbe, N., Campbell, A. E., Jackson, R., & Bennett, D. (2021) · The Journal of Cell Biology · doi:10.1083/jcb.202007005 · Cited by 12

Two neuronal peptides encoded from a single transcript regulate mitochondrial complex III in Drosophila

Bosch, J. A., Uğur, B., Pichardo‐Casas, I., Rabasco, J. T., Escobedo, F., Zuo, Z., Brown, B., Celniker, S., Sinclair, D. A., Bellen, H. J., et al. (2022) · eLife · doi:10.7554/elife.82709 · Cited by 12

Cellular compartmentalisation and receptor promiscuity as a strategy for accurate and robust inference of position during morphogenesis

Iyer, K. S., Prabhakara, C., Mayor, S., & Rao, M. (2023) · eLife · doi:10.7554/elife.79257 · Cited by 12

tgCRISPRi: efficient gene knock-down using truncated gRNAs and catalytically active Cas9

Auradkar, A., Guichard, A., Kaduwal, S., Sneider, M., & Bier, E. (2023) · Nature Communications · doi:10.1038/s41467-023-40836-3 · Cited by 12

An introduction to genome editing CRISPR-Cas systems

Singh, V. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-818140-9.00001-5 · Cited by 14

A Drosophila model to study retinitis pigmentosa pathology associated with mutations in the core splicing factor Prp8

Stanković, D., Claudius, A.-K., Schertel, T., Bresser, T., & Uhlířová, M. (2020) · Disease Models & Mechanisms · doi:10.1242/dmm.043174 · Cited by 11

A Nucleolar Isoform of the Drosophila Ubiquitin Specific Protease dUSP36 Regulates MYC-Dependent Cell Growth

Thevenon, D., Seffouh, I., Pillet, C., Crespo-Yàñez, X., Fauvarque, M., & Taillebourg, E. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00506 · Cited by 12

Postsynaptic cAMP signalling regulates the antagonistic balance of Drosophila glutamate receptor subtypes

Zhao, K., Hong, H., Zhao, L., Huang, S., Gao, Y., Metwally, E., Jiang, Y., Sigrist, S. J., & Zhang, Y. (2020) · Development · doi:10.1242/dev.191874 · Cited by 10

Interplay between axonal Wnt5-Vang and dendritic Wnt5-Drl/Ryk signaling controls glomerular patterning in the Drosophila antennal lobe

Hing, H. K., Snyder, J., Reger, N., & Fradkin, L. G. (2020) · PLoS Genetics · doi:10.1371/journal.pgen.1008767 · Cited by 15

De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features

Pan, X., Tao, A. M., Lu, S., Ma, M., Hannan, S. B., Slaugh, R., Williams, S. D., O’Grady, L., Kanca, O., Person, R., et al. (2024) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2024.02.007 · Cited by 12

Expanding the CRISPR base editing toolbox in Drosophila melanogaster

Clark, M., Nguyen, C., Nguyen, H., Tay, A. P., Beach, S. J., Maselko, M., & Amo, V. L. D. (2024) · Communications Biology · doi:10.1038/s42003-024-06848-5 · Cited by 11

Quantitative analysis of cell shape and the cytoskeleton in developmental biology

Yevick, H. G., & Martin, A. C. (2018) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.333 · Cited by 11

Targeted substrate degradation by Kelch controls the actin cytoskeleton during ring canal expansion

Hudson, A. M., Mannix, K. M., Gerdes, J. A., Kottemann, M. C., & Cooley, L. (2018) · Development · doi:10.1242/dev.169219 · Cited by 11

Chromosome Preference During Homologous Recombination Repair of DNA Double-Strand Breaks inDrosophila melanogaster

Fernandez, J., Bloomer, H., Kellam, N., & LaRocque, J. R. (2019) · G3 Genes Genomes Genetics · doi:10.1534/g3.119.400607 · Cited by 11

Gelsolin and dCryAB act downstream of muscle identity genes and contribute to preventing muscle splitting and branching in Drosophila

Bertin, B., Renaud, Y., Jagla, T., Lavergne, G., Dondi, C., Ponte, J. P. D., Junion, G., & Jagla, K. (2021) · Scientific Reports · doi:10.1038/s41598-021-92506-3 · Cited by 11

Novel function of N -acetyltransferase for microtubule stability and JNK signaling in Drosophila organ development

Mok, J.-W., & Choi, K. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2010140118 · Cited by 11

Loss of the D β 1 nicotinic acetylcholine receptor subunit disrupts bursicon -driven wing expansion and diminishes adult viability in Drosophila melanogaster

Christesen, D., Yang, Y. T., Chen, W., Batterham, P., & Perry, T. (2021) · Genetics · doi:10.1093/genetics/iyab112 · Cited by 11

Base Editing of Somatic Cells Using CRISPR–Cas9 in Drosophila

Marr, E. E., & Potter, C. J. (2021) · The CRISPR Journal · doi:10.1089/crispr.2021.0062 · Cited by 11

A conditional glutamatergic synaptic vesicle marker forDrosophila

Certel, S. J., Ruchti, E., McCabe, B. D., & Stowers, R. S. (2022) · G3 Genes Genomes Genetics · doi:10.1093/g3journal/jkab453 · Cited by 11

Intronic gRNAs for the Construction of Minimal Gene Drive Systems

Nash, A., Capriotti, P., Hoermann, A., Papathanos, P. A., & Windbichler, N. (2022) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2022.857460 · Cited by 11

HEATR5B associates with dynein‐dynactin and promotes motility of AP1‐bound endosomal membranes

Madan, V., Albacete-Albacete, L., Jin, L., Scaturro, P., Watson, J. L., Muschalik, N., Begum, F., Boulanger, J., Bauer, K. F., Kiebler, M. A., et al. (2023) · The EMBO Journal · doi:10.15252/embj.2023114473 · Cited by 10

Usp14 is required for spermatogenesis and ubiquitin stress responses in Drosophila melanogaster

Kovács, L., Nagy, Á., Pál, M., & Deák, P. (2020) · Journal of Cell Science · doi:10.1242/jcs.237511 · Cited by 11

Nucleolar stress in Drosophila neuroblasts, a model for human ribosomopathies

Baral, S. S., Lieux, M. E., & DiMario, P. J. (2020) · Biology Open · doi:10.1242/bio.046565 · Cited by 15

High-Temporal-Resolution smFISH Method for Gene Expression Studies in Caenorhabditis elegans Embryos

Charles, S., Aubry, G., Chou, H. T., Paaby, A. B., & Lu, H. (2020) · Analytical Chemistry · doi:10.1021/acs.analchem.0c02966 · Cited by 11

Genome editing efficiency of four Drosophila suzukii endogenous U6 promoters

Ni, X., Lu, W. ‐., Qiao, X., & Huang, J. (2021) · Insect Molecular Biology · doi:10.1111/imb.12707 · Cited by 11

The application of somatic CRISPR‐Cas9 to conditional genome editing in Caenorhabditis elegans

Li, W., & Ou, G. (2016) · genesis · doi:10.1002/dvg.22932 · Cited by 11

Synaptic deregulation of cholinergic projection neurons causes olfactory dysfunction across five fly Parkinsonism models

Pech, U., Janssens, J., Schoovaerts, N., Kuenen, S., Calatayud, C., Gallego, S. F., Makhzami, S., Hulselmans, G. J., Poovathingal, S. K., Davie, K., et al. (2024) · eLife · doi:10.1101/2023.03.11.532176 · Cited by 18

A small-molecule approach to restore female sterility phenotype targeted by a homing suppression gene drive in the fruit pest Drosophila suzukii

Ma, S., Ni, X., Chen, S., Qiao, X., Xu, X., Chen, W., Champer, J., & Huang, J. (2024) · PLoS Genetics · doi:10.1371/journal.pgen.1011226 · Cited by 10

Toll-1-dependent immune evasion induced by fungal infection leads to cell loss in the Drosophila brain

Singh, D. N., Roberts, A. R. E., Wang, X., Li, G., Moraga, E. Q., Alliband, D., Ballou, E. R., Tsai, H.-J., & Hidalgo, A. (2025) · PLoS Biology · doi:10.1371/journal.pbio.3003020 · Cited by 10

Rho/Rok-dependent regulation of actomyosin contractility at tricellular junctions restricts epithelial permeability in Drosophila

Jacobs, T., Sanchez, J. I., Reger, S., & Luschnig, S. (2025) · Current Biology · doi:10.1016/j.cub.2025.01.043 · Cited by 12

Olfactory projection neuron rewiring in the brain of an ecological specialist

Dürr, B. R., Bertolini, E., Takagi, S., Pascual, J., Abuin, L., Lucarelli, G., Benton, R., & Auer, T. O. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115615 · Cited by 10

Cross-species implementation of an innate courtship behavior by manipulation of the sex-determinant gene

Tanaka, R., Hara, Y., Sato, K., Kohatsu, S., Murakami, H., Higuchi, T., Awasaki, T., Kondo, S., Toyoda, A., Kamikouchi, A., et al. (2025) · Science · doi:10.1126/science.adp5831 · Cited by 8

Retinal calcium waves coordinate uniform tissue patterning of the Drosophila eye

Choi, B. J., Chen, Y., & Desplan, C. (2025) · Science · doi:10.1126/science.ady5541 · Cited by 8

Intimate functional interactions between TGS1 and the Smn complex revealed by an analysis of the Drosophila eye development

Maccallini, P., Bavasso, F., Scatolini, L., Bucciarelli, E., Noviello, G., Lisi, V., Palumbo, V., D’Angeli, S., Cacchione, S., Cenci, G., et al. (2020) · PLoS Genetics · doi:10.1371/journal.pgen.1008815 · Cited by 10

Efficient CRISPR Mutagenesis in Sturgeon Demonstrates Its Utility in Large, Slow-Maturing Vertebrates

Štundl, J., Soukup, V., Franěk, R., Pospíšilová, A., Psutkova, V., Pšenička, M., Cerny, R., Bronner-Fraser, M. E., Medeiros, D. M., & Jandzík, D. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.750833 · Cited by 11

Fluorescent labeling of genomic loci in Drosophila imaginal discs with heterologous DNA-binding proteins

Delker, R. K., Munce, R. H., Hu, M., & Mann, R. S. (2022) · Cell Reports Methods · doi:10.1016/j.crmeth.2022.100175 · Cited by 12

Single-nucleus RNA-sequencing in pre-cellularization Drosophila melanogaster embryos

Albright, A., Stadler, M. R., & Eisen, M. B. (2022) · PLoS ONE · doi:10.1371/journal.pone.0270471 · Cited by 8

Genome editing of the vermilion locus generates a visible eye color marker for Oncopeltus fasciatus

Reding, K., Lê, M., & Pick, L. (2023) · Scientific Reports · doi:10.1038/s41598-023-31145-2 · Cited by 10

The oxoglutarate dehydrogenase complex is involved in myofibril growth and Z-disc assembly in Drosophila

González‐Morales, N., Marescal, O., Szikora, S., Katzemich, A. R., Correia‐Mesquita, T. O., Bíró, P., Erdélyi, M., Mihály, J., & Schöck, F. (2023) · Journal of Cell Science · doi:10.1242/jcs.260717 · Cited by 10

From Reductionism to Holism: Toward a More Complete View of Development Through Genome Engineering

Delker, R. K., & Mann, R. S. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-63904-8_3 · Cited by 10

A pipeline for precise and efficient genome editing by sgRNA-Cas9 RNPs in Drosophila

Nyberg, K. G., Nguyen, J. Q., Kwon, Y.-J., Blythe, S. A., Beitel, G. J., & Carthew, R. W. (2020) · Fly · doi:10.1080/19336934.2020.1832416 · Cited by 10

Rpd3/CoRest-mediated activity-dependent transcription regulates the flexibility in memory updating in Drosophila

Takakura, M., Nakagawa, R., Ota, T., Kimura, Y., Ng, M. Y., Alia, A. G. M., Okuno, H., & Hirano, Y. (2021) · Nature Communications · doi:10.1038/s41467-021-20898-x · Cited by 10

Identification of additional dye tracers for measuring solid food intake and food preference via consumption-excretion in Drosophila

Shell, B. C., & Grotewiel, M. (2022) · Scientific Reports · doi:10.1038/s41598-022-10252-6 · Cited by 10

CRISPR-Cas-Induced Mutants Identify a Requirement for dSTIM in Larval Dopaminergic Cells of Drosophila melanogaster

Pathak, T., Trivedi, D., & Hasan, G. (2017) · G3 Genes Genomes Genetics · doi:10.1534/g3.116.038539 · Cited by 9

CRISPR-based gene replacement reveals evolutionarily conserved axon guidance functions of Drosophila Robo3 and Tribolium Robo2/3

Evans, T. A. (2017) · EvoDevo · doi:10.1186/s13227-017-0073-y · Cited by 10

A Cut/cohesin axis alters the chromatin landscape to facilitate neuroblast death

Arya, R., Gyonjyan, S., Harding, K. W., Sarkissian, T., Li, Y., Zhou, L. J., & White, K. (2019) · Development · doi:10.1242/dev.166603 · Cited by 10

Tunable Transcriptional Interference at the Endogenous Alcohol Dehydrogenase Gene Locus in Drosophila melanogaster

Jorgensen, V., Chen, J., Wende, H. V., Harris, D. E., McCarthy, A., Breznak, S. M., Wong-Deyrup, S. W., Chen, Y., Rangan, P., Brar, G. A., et al. (2020) · G3 Genes Genomes Genetics · doi:10.1534/g3.119.400937 · Cited by 10

Condensin I is required for faithful meiosis in Drosophila males

Kleinschnitz, K., Vießmann, N., Jordan, M. A., & Heidmann, S. K. (2020) · Chromosoma · doi:10.1007/s00412-020-00733-w · Cited by 9

FGF Pyramus Has a Transmembrane Domain and Cell-Autonomous Function in Polarity

Stepanik, V. A., Sun, J., & Stathopoulos, A. (2020) · Current Biology · doi:10.1016/j.cub.2020.06.006 · Cited by 10

Competition between two phosphatases fine-tunes Hedgehog signaling

Liu, M., Liu, A., Wang, J., Zhang, Y., Li, Y., Su, Y., & Zhu, A. J. (2020) · The Journal of Cell Biology · doi:10.1083/jcb.202010078 · Cited by 10

The Slit‐binding Ig1 domain is required for multiple axon guidance activities of Drosophila Robo2

Howard, L. J., Reichert, M. C., & Evans, T. A. (2021) · genesis · doi:10.1002/dvg.23443 · Cited by 10

Powerful, efficient QTL mapping in Drosophila melanogaster using bulked phenotyping and pooled sequencing

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